Lv1
31 积分 2021-10-11 加入
Identification of a Patient with Transfusion-Dependent β-Thalassemia Caused by Compound Heterozygous Mutations of HBB: C.84_85insC and Common Linked Intronic Variants in HBB
19小时前
求助中
Pre- and postantibiotic epoch: The historical spread of antimicrobial resistance
1个月前
已完结
Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing
2个月前
已完结
Sequencing of 50 Human Exomes Reveals Adaptation to High Altitude
2个月前
已完结
Familial hypercholesterolemia: epidemiology, Neolithic origins and modern geographic distribution
4个月前
已完结
Hereditary Hemochromatosis
4个月前
已完结
Mutation spectrum of MMACHC in Chinese pediatric patients with cobalamin C disease: A case series and literature review
4个月前
已完结
Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management
4个月前
已完结
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
5个月前
已完结
Whole-genome Sequencing Association Analysis of Quantitative Platelet Traits in A Large Cohort of β-thalassemia
5个月前
已完结
皖公网安备34019202002308
